scholarly journals Separation of tungsten and rhenium on alumina

2004 ◽  
Vol 69 (8-9) ◽  
pp. 683-688 ◽  
Author(s):  
Jurij Vucina ◽  
Dagoljub Lukic ◽  
Milovan Stoiljkovic
Keyword(s):  
Nitric Acid ◽  
Sodium Chloride ◽  
Aqueous Phase ◽  
Aqueous Media ◽  
Distribution Coefficients ◽  
Experimental Conditions ◽  
Efficient Separation ◽  
Separation Factors ◽  
Ph Range

The conditions for the efficient separation of tungsten(VI) and rhenium (VII) on alumina were established. The distribution coefficients K d for tungstate and perrhenate anions, as well as the separation factors ?(? = KdWO42-/Kd ReO4-) were determined using hydrochloric or nitric acid as the aqueous media. Asolution of sodium chloride in the pH range 2?6 was also examined. Under all the tested experimental conditions, alumina is a much better adsorbent for tungsten than for rhenium. The obtained results indicated that the best separation of these two elements is achieved when 0.01? 0.1 mol dm-3HCl or 1.0mol dm-3 HNO3 are used as the aqueous media. If NaCl is used as the aqueous phase, the best separation is achieved with 0.20 mol dm-3 NaCl pH 4?6. Under these experimental conditions, the breakthrough and saturation capacities of alumina for tungsten at pH4 are 17 and 26 mg W/g Al2O3 respectively. With increasing pH, these values decrease. Thus, at pH 6 they are only 4 and 13 mg W/g Al2O3, respectively.

scholarly journals THE INACTIVATION OF DILUTE SOLUTIONS OF CRYSTALLINE TRYPSIN BY X-RADIATION

1955 ◽  
Vol 38 (5) ◽  
pp. 581-598 ◽  
Author(s):  
Margaret R. McDonald
Keyword(s):  
Sulfuric Acid ◽  
Nitric Acid ◽  
Hydrochloric Acid ◽  
Radiation Effects ◽  
Reaction Yield ◽  
X Rays ◽  
Dilute Solutions ◽  
Experimental Conditions ◽  
Ph Range ◽  
Ph Curve

The proteolytic activity of dilute solutions of clystalline trypsin is destroyed by x-rays, the amount of inactivation being an exponential function of the radiation dose. The reaction yield increases steadily with increasing concentration of trypsin, varying, as the concentration of enzyme is increased from 1 to 300 µM, from 0.068 to 0.958 micromole of trypsin per liter inactivated per 1000 r with 0.005 N hydrochloric acid as the solvent, from 0.273 to 0.866 with 0.005 N sulfuric acid as the solvent, and from 0.343 to 0.844 with 0.005 N nitric acid as the solvent. When the reaction yields are plotted as a function of the initial concentration of trypsin, they fall on a curve given by the expression Y α XK, in which Y is the reaction yield, X is the concentration of trypsin, and K is a constant equal to 0.46, 0.20, and 0.16, respectively, with 0.005 N hydrochloric, sulfuric, and nitric acids as solvents. The differences between the reaction yields found with chloride and sulfate ions in I to 10 µM trypsin solutions are significant only in the pH range from 2 to 4. The amount of inactivation obtained with a given dose of x-rays depends on the pH of the solution being irradiated and the nature of the solvent. The reaction yield-pH curve is a symmetrical one, with minimum yields at about pH 7. Buffers such as acetate, citrate, borate and barbiturate, and other organic molecules such as ethanol and glucose, in concentrations as low as 20 µM, inhibit the inactivation of trypsin by x-radiation. Sigmoid inactivation-dose curves instead of exponential ones are obtained in the presence of ethanol. The reaction yields for the inactivation of trypsin solutions by x-rays are approximately 1.5 times greater when the irradiation is done at 26°C. than when it is done at 5°C., when 0.005 N hydrochloric acid is the solvent. The dependence on temperature is less when 0.005 N sulfuric acid is used, and is negligible with 0.005 N nitric acid. The difficulties involved in interpreting radiation effects in aqueous systems, and in comparing the results obtained under different experimental conditions, are discussed.

Extraction of americium with benzyldibutylamine from nitrate solutions

1979 ◽  
Vol 44 (8) ◽  
pp. 2366-2372 ◽  
Author(s):  
Věra Jedináková ◽  
Jana Cibulková ◽  
Libor Kuča
Keyword(s):  
Nitric Acid ◽  
Chemical Analysis ◽  
Ir Spectra ◽  
Aqueous Phase ◽  
Organic Phase ◽  
Nuclear Fission ◽  
Salting Out ◽  
Nitrate Medium ◽  
Separation Factors ◽  
Nitrate Solutions

The extraction of Am(III) with benzyldibutylamine from nitrate medium was examined in dependence on the concentration of nitric acid, kind and concentration of the salting-out agent in the aqueous phase, and on the solvent. Am(III) is extracted into the organic phase in the form of {(R3NH+)α, Am(NO3)52-}. The IR spectra of the organic phase are discussed and confronted with the results of the chemical analysis of the organic phase. The extraction of Am(III) and of lanthanoids was found to be considerably higher than that of some products of corrosion and nuclear fission (Cs, Sr, Zr, Fe), which is documented by the high values of the separation factors.

scholarly journals Column Separation of Am(III) and Eu(III) by α-Zirconium Phosphate Ion Exchanger in Nitric Acid

2020 ◽  
Vol 4 (1) ◽  
pp. 14
Author(s):  
Elmo W. Wiikinkoski ◽  
Iiro Rautsola ◽  
Junhua Xu ◽  
Risto Koivula
Keyword(s):  
Zirconium Phosphate ◽  
Distribution Coefficients ◽  
Ion Exchanger ◽  
Molar Ratio ◽  
Experimental Conditions ◽  
Column Separation ◽  
Phosphate Ion ◽  
Trivalent Lanthanide ◽  
Separation Factors ◽  
Equimolar Solution

The trivalent lanthanide-actinide separations are a major challenge in reprocessing of nuclear fuels. To achieve this, commonly organic extractants and solvents are utilized in elaborate processes. Here we report a simple new method that can perform a supportive or alternative role. A nanocrystalline α-zirconium phosphate ion exchanger was utilized for Eu(III)/Am(III) column separation. Comprehensive preliminary studies were done using batch experiments to optimize the final separation conditions. The distribution coefficients for Eu were determined as a function of pH (from 0 to 3) and salinity (Na, Sr). The distribution coefficients for Am were determined as a function of pH, and Eu concentration, from 1:40 to 10,000:1 Eu:Am molar ratio. The exchanger always preferred Eu over Am in our experimental conditions. Separation factors (Eu:Am) of up to 400 were achieved in binary Eu-Am solution in pH 1. The breakthrough capacity was determined in dynamic column conditions using Eu: 0.3 meq∙g−1, which is approximately 4% of the theoretical maximum capacity. Two types of hot column separation tests were conducted: (i) binary load (selective Am elution), and (ii) continuous equimolar binary feed. In both cases separation was achieved. In (i), the majority (82% of the recovered 93%) of Am could be purified from Eu with extremely high 99.999% molar purity, while alternatively even more (95% of the recovered 93%) at a lower purity of 99.7 mol %. In (ii), up to 330 L∙kg−1 of the equimolar solution per mass of the exchanger could be treated with Am purity above 99.5 mol % in the total eluate. Alternatively, up to 630 L∙kg−1 above 95 mol %, or up to 800 L∙kg−1 above 90 mol % purities.

EFFECT OF REDUCING AGENTS ON THE VIABILITY OF EQUINE ENCEPHALOMYELITIS VIRUS (EASTERN TYPE)

1946 ◽  
Vol 24e (4) ◽  
pp. 119-133
Author(s):  
N. A. Labzoffsky
Keyword(s):  
Sodium Chloride ◽  
Reducing Agents ◽  
Present Communication ◽  
Virus Suspension ◽  
Experimental Conditions ◽  
Cysteine Hydrochloride ◽  
Wide Range ◽  
Encephalomyelitis Virus ◽  
Ph Range

The present communication deals with the effect of reducing agents (cysteine hydrochloride, sodium thioglycollate, and sodium formaldehyde sulphoxylate) on the viability of equine encephalomyelitis virus (Eastern type). Cysteine hydrochloride was found to be a valuable reagent in in vitro studies of equine encephalomyelitis virus, because it greatly retards loss of infectivity of the virus under experimental conditions. It was observed that a virus suspension containing cysteine hydrochloride (1:1000) remained infective after exposure to 37 °C. for 14 days, although the guinea-pig titre was reduced from 1:108 to 1:102. The same reduction in the titre of virus suspended in buffered 0.85% sodium chloride solution occurred after exposure to 37 °C. for 120 hr. only, and in unbuffered 0.85% sodium chloride after 24 hr. exposure. Further, equine encephalomyelitis virus, in the presence of cysteine hydrochloride, retains its infectivity without demonstrable loss, over a pH range between 4.8 and 8.2 for 48 hr. at 37 °C. The titre of equine encephalomyelitis virus is maintained at 37 °C. for 48 hr. in a rather wide range of Eh, created with the aid of cysteine hydrochloride, at least in the range between − 0.151 and + 0.02 volts. On the other hand, addition of sodium formaldehyde sulphoxylate or sodium thioglycollate to a suspension of equine encephalomyelitis virus does not retard loss of infectivity of the virus. These reagents, therefore, are not suitable for the conservation of infectivity of the virus in vitro.

THE EXTRACTION OF THORIUM AND SOME LOWER LANTHANIDE NITRATES BY DIBUTYL BUTYL PHOSPHONATE

1962 ◽  
Vol 40 (8) ◽  
pp. 1684-1689 ◽  
Author(s):  
P. G. Manning
Keyword(s):  
Nitric Acid ◽  
National Laboratory ◽  
Nitric Acid Concentration ◽  
Distribution Coefficients ◽  
Metal Species ◽  
Trace Metal Concentration ◽  
Oak Ridge ◽  
Separation Factors ◽  
Lanthanide Nitrates ◽  
Aqueous Nitric Acid

The distribution of thorium and a number of lanthanides between nitric acid and solutions of dibutyl butyl phosphonate in odorless kerosene has been examined as a function of the aqueous nitric acid concentration. Experiments were conducted at trace metal concentration using radioisotopes. Separation factors (denoted by S and defined as the ratio of the distribution coefficients, K, for two metal species) have been measured for some lanthanide–lanthanide couples and also for some thorium–lanthanide couples. Results indicate that separation factors between successive lanthanides (given by S = KZ+1/KZ) at the lower end of the rare-earth series are superior to those obtained with either tributyl phosphate (TBP) (D. Scargill et al. J. Inorg. & Nuclear Chem. 4, 304 (1957)) or trioctyl phosphine oxide (TOPO) (J. M. Schmitt. Oak Ridge National Laboratory. Unpublished data), but as Z increases, SDBBP ~STBP > STOPO. For thorium–lanthanide couples, S′DBBP > S′TBP. Measurements over a range of extractant concentrations indicate that the lanthanides are extracted as trisolvates.

scholarly journals Solvent extraction of europium(III) from technogenic solutions with the use of surfactants

2020 ◽  
Vol 15 (4) ◽  
pp. 51-58
Author(s):  
N. V. Dzhevaga ◽  
O. L. Lobacheva
Keyword(s):  
Rare Earth ◽  
Nitric Acid ◽  
Aqueous Phase ◽  
Ph Value ◽  
Rare Earth Metals ◽  
Target Component ◽  
Acid Solutions ◽  
Extraction And Separation ◽  
Nitric Acid Solutions ◽  
Ph Range

Objectives. The extraction and separation of rare-earth metals is a complicated process that requires a multidisciplinary and detailed investigation. Liquid-liquid extraction with the use of surfactant, along with the thermodynamic analysis of the parameters is considered a promising approach. The extraction and separation of rare-earth metals from low-concentration solutions represents an attractive research opportunity. The extraction of europium(III) from nitric acid solutions in the form of dodecyl sulfates has been experimentally studied. This work focuses on the study of fundamental and alternative sources of rare-earth metals and their extraction and separation.Methods. The extraction was performed on a top drive ES-8300 D equipment for 30 min at about 700 rpm. Infrared spectroscopy (Nicolet 6700 spectrometer) was used to determine the type of salts extracted into the organic phase. Extraction was studied in solutions with single cations and with a combination of the target element and interfering cations. For the latter, the concentrations of extracted elements in the aqueous phase were determined by optical emission spectroscopy with inductively coupled plasma on an ICPE-9000 (Shimadzu) spectrometer. The spectrometer was calibrated using standard samples for ICP CertiPUR (Merck).Results. The dependence of the distribution and separation coefficients of rare-earth metals during extraction on the pH value of the aqueous phase at equilibrium was investigated. Moreover, the form in which the elements are extracted was analyzed based on thermodynamic parameters. The minimum concentration of the target component in the aqueous phase was observed at pH 4.0. In general, the dependence of the distribution coefficient on the pH value of the medium is poorly expressed over the entire range of the pH range of the water phase. Based on the spectra of spent and pure isooctyl alcohol, it was concluded that europium dodecyl sulfates are extracted into the organic phase as Eu(C12H25OSO3) 3 solvates.Conclusions. The extraction of europium(III) from nitric acid solutions in the form of dodecyl sulfates was demonstrated. The advantages of the proposed method are the possibility of selective extraction of the target component from dilute solutions and the use of an easily available surfactant (sodium dodecyl sulfate). The efficiency of extraction of europium dodecyl sulfates was maximal in the pH range from 2.0 to 7.5, which reflects a weak dependence on the acidity of the aqueous phase. In addition, in the highly alkaline pH region, the extraction efficiency is reduced.

Extraction of Am(III) by benzyldibutylamine from nitrate solutions of lanthanides

1981 ◽  
Vol 46 (1) ◽  
pp. 194-200 ◽  
Author(s):  
Marta Vojtíšková ◽  
Věra Jedináková ◽  
Libor Kuča
Keyword(s):  
Nitric Acid ◽  
Nuclear Fuel ◽  
Organic Phase ◽  
Spent Nuclear Fuel ◽  
Optimum Conditions ◽  
Separation Factors ◽  
Nitrate Solutions

Benzyldibutylamine is a suitable extractant for the separation of Am(III) and Ln(III) from the acidic nitrate solutions. The effect of lanthanides and yttrium on the extraction of Am(III) has been followed under the conditions modelling the content of these components in the spent nuclear fuel. The separation factors αAm/Ln were evaluated for the optimum conditions found for the separation of Am(III) from the lanthanides. The coextraction of nitric acid and water into the organic phase is discussed.

scholarly journals Nitration of Jharia basin coals, India: a study of structural modifications by XRD and FTIR techniques

2021 ◽  
Author(s):  
Prabal Boral ◽  
Atul K. Varma ◽  
Sudip Maity
Keyword(s):  
Acetic Acid ◽  
Nitric Acid ◽  
Linear Relationship ◽  
Glacial Acetic Acid ◽  
Vitrinite Reflectance ◽  
Aqueous Media ◽  
Interlayer Spacing ◽  
Acetic Acid Medium ◽  
X Ray ◽  
The Media

AbstractFour coal samples from Jharia basin, India are treated with nitric acid in glacial acetic acid and aqueous media to find out the chemical, petrographic and spatial structure of the organic mass by X-ray diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FTIR) techniques. X-ray parameters of coal like interlayer spacing (d002), crystallite size (Lc), aroamticity (fa), average number of aromatic layers (Nc), and coal rank (I26/I20) have been determined using profile-fitting software. Considerable variation is observed in treated coals in comparison to the demineralized coals. The d002 values of treated coals have increased in both the media showing increase in disordering of organic moieties. A linear relationship has been observed between d002 values with the volatile matter of the coals. Similarly, the d002 values show linear relationship with Cdmf contents for demineralized as well as for the treated coals in both the media. The Lc and Nc values have decreased in treated coals corresponding to demineralized coals. The present study shows that nitration in both the media is capable of removing the aliphatic side chains from the coals and aromaticity (fa) increases with increase in rank and shows a linear relationship with the vitrinite reflectance. The corresponding I26/I20 values are least for treated coals in glacial acetic acid medium followed by raw and then to treated coals in aqueous medium. FTIR studies show that coal arenes of the raw coals are converted into nitro-arenes in structurally modified coals (SMCs) in both the media, the corresponding bands at 1550–1490 and 1355–1315 cm−1 respectively. FTIR study confirms that nitration is the predominant phenomenon, though, oxidation and nitration phenomena takes place simultaneously during treatment with nitric acid to form SMCs. In comparison to raw coals, the SMCs show higher aromaticity and may be easily converted to coal derived products like activated carbon and specialty carbon materials.

Efficient trace-scale extraction method of reactor produced 199Au adequate for nuclear medicine applications

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mohamed F. Attallah ◽  
Ahmed M. Shahr El-Din ◽  
Mohamed A. Gizawy ◽  
Amal M. I. Ali
Keyword(s):  
Aqueous Media ◽  
Selective Extraction ◽  
Extraction Process ◽  
High Yield ◽  
High Recovery ◽  
Rapid Separation ◽  
Efficient Separation ◽  
Liquid Liquid Extraction ◽  
Cyanex 302 ◽  
Cyanex 923

Abstract Production of no carrier-added (NCA) 199Au through natPt(n, γ) reaction and subsequent purification using liquid-liquid extraction from other radioisotopes is studied in the context of theranostic application. Comparative separation of NCA 199Au after dissolution of activated Pt target using three Cyanex compounds (Cyanex-272, Cyanex-302 and Cyanex-923) is evaluated. The extraction process is optimized in terms of the type of extractant, the concentration of extractant, extraction time and aqueous media (HNO3, NH4OH). Among these extractants, the Cynaex-923 is efficient and promising for rapid separation and production of NCA 199Au from HNO3 by high extraction %. Selective extraction of 199Au from other Pt and Ir radioisotopes is observed. High recovery of 199Au was obtained in the case of Cyanex-923 using 0.05 M thiourea dissolved in HCl or 2 M NaOH. Our results find the Cyanex-923 as a promising extractant for efficient separation of 199Au from irradiated Pt target with high yield (99%).

Sign in / Sign up

Export Citation Format

Share Document